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rs10520873

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs10520873(A;G)
Make rs10520873(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position7901117
GeneMTRR
is asnp
is mentioned by
dbSNPrs10520873
dbSNP (old)rs10520873
ClinGenrs10520873
ebirs10520873
HLIrs10520873
Exacrs10520873
Gnomadrs10520873
Varsomers10520873
Maprs10520873
PheGenIrs10520873
Biobankrs10520873
1000 genomesrs10520873
hgdprs10520873
ensemblrs10520873
gopubmedrs10520873
geneviewrs10520873
scholarrs10520873
googlers10520873
pharmgkbrs10520873
gwascentralrs10520873
openSNPrs10520873
23andMers10520873
23andMe allrs10520873
SNP Nexus

SNPshotrs10520873
SNPdbers10520873
MSV3drs10520873
GWAS Ctlgrs10520873
GMAF0.1997
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20883119] Common polymorphisms in six genes of the methyl group metabolism pathway and obesity in European adolescents


ClinVar
Risk rs10520873(G;G)
Alt rs10520873(G;G)
Reference Rs10520873(A;A)
Significance Non-pathogenic
Disease Disorders of Intracellular Cobalamin Metabolism
Variation info
Gene MTRR
CLNDBN Disorders of Intracellular Cobalamin Metabolism
Reversed 1
HGVS NC_000005.9:g.7901230T>C
CLNSRC
CLNACC RCV000340298.1,